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HELMINTHOSPORIUM SOLANI - 0268-0906-50 - (HELMINTHOSPORIUM SOLANI)

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Drug Information of HELMINTHOSPORIUM SOLANI

Product NDC: 0268-0906
Proprietary Name: HELMINTHOSPORIUM SOLANI
Non Proprietary Name: HELMINTHOSPORIUM SOLANI
Active Ingredient(s): 20000    [PNU]/mL & nbsp;   HELMINTHOSPORIUM SOLANI
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of HELMINTHOSPORIUM SOLANI

Product NDC: 0268-0906
Labeler Name: ALK-Abello, Inc.
Product Type: NON-STANDARDIZED ALLERGENIC
FDA Application Number: BLA103753
Marketing Category: BLA
Start Marketing Date: 19650101

Package Information of HELMINTHOSPORIUM SOLANI

Package NDC: 0268-0906-50
Package Description: 50 mL in 1 VIAL, MULTI-DOSE (0268-0906-50)

NDC Information of HELMINTHOSPORIUM SOLANI

NDC Code 0268-0906-50
Proprietary Name HELMINTHOSPORIUM SOLANI
Package Description 50 mL in 1 VIAL, MULTI-DOSE (0268-0906-50)
Product NDC 0268-0906
Product Type Name NON-STANDARDIZED ALLERGENIC
Non Proprietary Name HELMINTHOSPORIUM SOLANI
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19650101
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name HELMINTHOSPORIUM SOLANI
Strength Number 20000
Strength Unit [PNU]/mL
Pharmaceutical Classes Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of HELMINTHOSPORIUM SOLANI


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